Organotellurium compounds: an overview of synthetic methodologies

References

Abe, M.; Hilmey, D. G.; Stilts, C. E.; Sukumaran, D. K.; Detty, M. R. 21-telluraporphyrins. 1. Impact of 21, 23-heteroatom interactions on electrochemical redox potentials, 125Te NMR spectra, and absorption spectra. Organometallics2002, 21, 2986–2992. https://doi.org/10.1021/om0202219.Search in Google Scholar

Al-Asadi, R. H.; Al-Masoudi, W. A.; Abdual-Rassol, K. S. Synthesis, biological activity and computational study of some new unsymmetrical organotellurium compounds derived from 2-amino-5-carboxyphenyl mercury (II) chloride. Asian J. Chem.2016;28. https://doi.org/10.14233/ajchem.2016.19139.Search in Google Scholar

Al-Fregi, A. A.; Al-Salami, B. K.; Al-Khazragie, Z. K.; Al-Rubaie, A. Z. Synthesis, characterization and antibacterial studies of some new tellurated azo compounds. Phosphorus, Sulfur, and Silicon Relat. Elem.2019, 194, 33–38. https://doi.org/10.1080/10426507.2018.1470179.Search in Google Scholar

Ali, S.; Riaz, A.; Nawaz, H.; Majeed, M. I.; Iqbal, M. A.; Bhatti, H. N.; Rashid, N.; Kashif, M.; Tahir, M.; Nasir, S. Raman spectral characterization of silver metal-based complexes of different benzimidazolium ligands. Spectrochim. Acta Mol. Biomol. Spectros.2020a, 232, 118162. https://doi.org/10.1016/j.saa.2020.118162.Search in Google Scholar

Ali, S.; Riaz, A.; Majeed, M.I.; Iqbal, M.A.; Bhatti, H.N.; Rashid, N.; Kashif, M.; Tahir, M.; Nasir, S.; Farooq, S. Raman spectroscopy along with principal component analysis for the confirmation of silver (I)-N-heterocyclic carbene complex formation. Spectrochim. Acta Mol. Biomol. Spectros.2020b, 228, 117851. https://doi.org/10.1016/j.saa.2019.117851.Search in Google Scholar

Al‐Masoudi, W. A.; Al‐Asadi, R. H.; Othman, R. M.; Al‐Masoudi, N. A. Synthesis, antimicrobial activity, computational and modeling studies of some new organotellurium compounds containing azomoities. Eur. J. Chem.2015, 6, 374–380.10.5155/eurjchem.6.4.374-380.1254Search in Google Scholar

Al-Rubaie, A. Z.; Fahad, T. A.; Al-Jadaan, S. A.; Aboud, N. A. Synthesis and characterization of 2, 7-dihydro-1H-dinaphtho [c, e] tellurepin: a new heterocyclic telluride. J. Organomet. Chem.2004, 689, 2377–2381. https://doi.org/10.1016/j.jorganchem.2004.04.028.Search in Google Scholar

Al‐Rubaie, A. Z.; Al‐Masoudi, W. A.; Al‐Jadaan, S. A.; Jalbout, A. F.; Hameed, A. J. Synthesis, characterization, and computational study of some new organotellurium compounds containing azomethine groups. Heteroat. Chem. Int. J.Main Group Elem.2008, 19, 307–315.10.1002/hc.20437Search in Google Scholar

Al‐Rubaie, A. Z.; Yosif, M. Y.; Asker, K. A. A new cyclic telluride. synthesis and reactions of 1, 3, 5, 6, 7, 8‐hexahydronaphtho [2, 3‐c] tellurophene. Heteroat. Chem.2017, 28, e21402.10.1002/hc.21402Search in Google Scholar

Angeli, A.; Tanini, D.; Capperucci, A.; Supuran, C. T. First evaluation of organotellurium derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors. Bioorg. Chem.2018, 76, 268–272. https://doi.org/10.1016/j.bioorg.2017.12.010.Search in Google Scholar

Annaka, T.; Nakata, N.; Ishii, A. Synthesis, Structures, and Temperature-Dependent Photoluminescence of 1, 4-Diphenyl-1-telluro-1, 3-butadiene Incorporated in a Dibenzobarrelene Skeleton and Derivatives. Organometallics2015, 34, 1272–1278. https://doi.org/10.1021/acs.organomet.5b00016.Search in Google Scholar

Atif, M.; Bhatti, H. N.; Iqbal, M. A.; Jamil, Y. In-situ approach for the synthesis of bromide-bridged mercury (II) N-heterocyclic carbene complexes. J. Coord. Chem.2020a, 1–12.10.1080/00958972.2020.1765337Search in Google Scholar

Atif, M.; Bhatti, H. N.; Haque, R. A.; Iqbal, M. A.; Khadeer, M. B. A.; Majid, A. M. S. A. Synthesis, structure, and anticancer activity of symmetrical and non-symmetrical silver (i)-n-heterocyclic carbene complexes. Appl. Biochem. Biotech.2020b, 1–19.10.1007/s12010-019-03186-9Search in Google Scholar PubMed

Avila, D. S.; Benedetto, A.; Au, C.; Manarin, F.; Erikson, K.; Soares, F. A.; Rocha, J. B. T.; Aschner, M. Organotellurium and organoselenium compounds attenuate Mn-induced toxicity in Caenorhabditis elegans by preventing oxidative stress. Free Rad. Biol. Med.2012, 52, 1903–1910. https://doi.org/10.1016/j.freeradbiomed.2012.02.044.Search in Google Scholar

Ba, L. A.; Döring, M.; Jamier, V.; Jacob, C. Tellurium: an element with great biological potency and potential. Org. Biomol. Chem.2010, 8, 4203–4216. https://doi.org/10.1039/c0ob00086h.Search in Google Scholar

Bassan, J.; Willis, L. M.; Vellanki, R. N.; Nguyen, A.; Edgar, L. J.; Wouters, B. G.; Nitz, M. TePhe, a tellurium-containing phenylalanine mimic, allows monitoring of protein synthesis in vivo with mass cytometry. Proc. Nat. Acad. Sci.2019, 116, 8155–8160. https://doi.org/10.1073/pnas.1821151116.Search in Google Scholar

Beckmann, J.; Bolsinger, J. The Photooxidation of Bis (8‐dimethylaminonaphthyl) Ditelluride. Z. Anorg. Allg. Chem.2011, 637, 29–30. https://doi.org/10.1002/zaac.201000343.Search in Google Scholar

Beckmann, J.; Bolsinger, J.; Duthie, A. New Insights into the Formation and Structure of Diaryl Tritellurides. Organometallics2009, 28, 4610–4612. https://doi.org/10.1021/om900494d.Search in Google Scholar

Beckmann, J.; Bolsinger, J.; Duthie, A.; Finke, P. Synthesis and structure of an intramolecularly coordinated diaryltelluronic acid and its dimethyl ester. Organometallics2011, 31, 289–293. https://doi.org/10.1021/om2008953.Search in Google Scholar

Bhasin, K.; , Singh, N.; , Doomra, S.; Arora, E.; Ram, G.; Singh, S.; Nagpal, Y.; Mehta, S.; Klapotke, T. Regioselective synthesis of bis (2-halo-3-pyridyl) dichalcogenides (E= S, Se and Te): directed ortho-lithiation of 2-halopyridines. Bioinorg. Chem. App.2007, 2007.10.1155/2007/69263Search in Google Scholar PubMed PubMed Central

Bhasin, K.; Arora, E.; Kaur, K.; Kang, S.-K.; Gobel, M.; Klapoetke, T.; Mehta, S. Preparation and characterization of bis [4-dimethylamino-2-pyrimidyl] dichalcogenides (S, Se, Te): X-ray crystal structure of bis [4-dimethylamino-2-pyrimidyl] diselenide and its physicochemical behavior in microemulsion media. Tetrahedron2009, 65, 247–252. https://doi.org/10.1016/j.tet.2008.10.069.Search in Google Scholar

Bhasin, K.; Pundir, S.; Neogy, S.; Mehta, D.; Mehta, S. Synthesis, characterisation and structural aspects of some symmetrical organotellurium halides based on Bis (2-(3, 5-dimethyl-1H-pyrazol-1-yl) ethyl) telluride. Phosphorus, Sulfur, and Silicon Relat. Elem.2018, 193, 273–279. https://doi.org/10.1080/10426507.2017.1399127.Search in Google Scholar

Brown, A.; Hill, A. R.; Boles, J. O. Assessing cell growth in a microtiter plate reader with selective pressure incorporation of unnatural selenium and tellurium containing amino acids. FASEB J.2019, 33, 461.4, 1_supplement.10.1096/fasebj.2019.33.1_supplement.461.4Search in Google Scholar

Brutchey, R. L. Diorganyl dichalcogenides as useful synthons for colloidal semiconductor nanocrystals. Acc. Chem. Res.2015, 48, 2918–2926. https://doi.org/10.1021/acs.accounts.5b00362.Search in Google Scholar

Cargnelutti, R.; Lang, E. S.; Back, D. F.; Schumacher, R. F. Electrophilic cyclization of homopropargyl tellurides: Synthesis and supramolecular structures of 2-aryl-3-iodo-1-phenyl-tellurophenium iodides and polyiodides. Polyhedron2014, 73, 45–50. https://doi.org/10.1016/j.poly.2014.02.013.Search in Google Scholar

Carrera, E. I.; Seferos, D. S. Ring opening of π-delocalized 2, 5-diphenyltellurophene by chemical or self-sensitized aerobic photooxidation. Organometallics2017, 36, 2612–2621. https://doi.org/10.1021/acs.organomet.7b00240.Search in Google Scholar

Cava-Montesinos, P.; Cervera, M. L.; Pastor, A.; de la Guardia, M. Hydride generation atomic fluorescence spectrometric determination of ultratraces of selenium and tellurium in cow milk. Anal. Chim. Acta2003, 481, 291–300. https://doi.org/10.1016/s0003-2670(03)00085-0.Search in Google Scholar

Chandrasekhar, V.; Thirumoorthi, R. 1, 1 ‘-ferrocenedicarboxylate-bridged redox-active organotin and-tellurium-containing 16-membered macrocycles: synthesis, structure, and electrochemistry. Organometallics2007, 26, 5415–5422. https://doi.org/10.1021/om700622r.Search in Google Scholar

Chandrasekhar, V.; Kumar, A.; Pandey, M. D.; Metre, R. K. Telluroxane-supported coordination ligands: Synthetic and structural aspects. Polyhedron2013, 52, 1362–1368. https://doi.org/10.1016/j.poly.2012.06.005.Search in Google Scholar

Chauhan, R. S.; Kedarnath, G.; Wadawale, A.; Munoz-Castro, A.; Arratia-Perez, R.; Jain, V. K.; Kaim, W. Tellurium (0) as a Ligand: Synthesis and Characterization of 2-Pyridyltellurolates of Platinum (II) and Structures of [Pt {2-Te-3-(R) C5H3N} 2Te (PR′ 3)](R= H or Me). Inorg. chem.2010, 49, 4179–4185. https://doi.org/10.1021/ic902347s.Search in Google Scholar

Chauhan, A. K.; Bharti, S. N.; Srivastava, R. C. Stereospecific chlorotelluration of terminal acetylenes. J. Organomet. Chem.2012, 708, 75–81. https://doi.org/10.1016/j.jorganchem.2012.02.025.Search in Google Scholar

Chivers, T.; Laitinen, R. S. Tellurium: a maverick among the chalcogens. Chem. Soc. Rev.2015, 44, 1725–1739. https://doi.org/10.1039/c4cs00434e.Search in Google Scholar

Clark, A. R.; Nair, R.; Fronczek, F. R.; Junk, T. Facile access to aryltellurium compounds from arylboronic acids. Tetrahedron Lett.2002, 43, 1387–1389. https://doi.org/10.1016/s0040-4039(02)00025-4.Search in Google Scholar

Cotero-Villegas, A. M.; Moya-Cabrera, M.; Jancik, V.; Pérez-Redondo, M. d. C.; Martínez-Salas, P.; Cea-Olivares, R. Synthesis and characterization of the first Te (IV) organometallic complexes with azepane-1-carbodithioate. Phosphorus, Sulfur, and Silicon Relat. Elem.2017, 192, 338–343. https://doi.org/10.1080/10426507.2016.1238472.Search in Google Scholar

Cui, Y-J; Hu, F; Jia, A-Q; Xin, Z.-F.; Zhang, Q.-F. Syntheses and molecular structures of organo-tellurium (IV) halides trans-[(Ph2Te)(μ-Cl) 2] n, cis-[(Ph2Te)(μ-Cl) 2] n,[(p-MeC6H4) 2TeBr2], and [{(p-MeC6H4) 2TeBr} 2 (μ-O)]. J. Coord. Chem.2018, 71, 2183–2193. https://doi.org/10.1080/00958972.2018.1478085.Search in Google Scholar

Cunha, RL; Omori ÁT; Castelani, P. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step. J. Organomet. Chem.2004, 689, 3631–3636. https://doi.org/10.1016/j.jorganchem.2004.08.041.Search in Google Scholar

Cunha, R. L.; Urano, M. E.; Chagas, J. R. Tellurium-based cysteine protease inhibitors: evaluation of novel organotellurium (IV) compounds as inhibitors of human cathepsin B. Bioorg. Med. Chem. Lett.2005, 15, 755–760. https://doi.org/10.1016/j.bmcl.2004.11.012.Search in Google Scholar

Cunha, R. L.; Gouvea, I. E.; Juliano, L. A glimpse on biological activities of tellurium compounds. An Acad. Bras Ciências2009, 81, 393–407. https://doi.org/10.1590/s0001-37652009000300006.Search in Google Scholar

D’Arcy, K.; Doyle, A. P.; Kavanagh, K.; Ronconi, L.; Fresch, B.; Montagner, D. Stability of antibacterial Te (IV) compounds: a combined experimental and computational study. J. Inorg. Biochem.2019, 110719. https://doi.org/10.1016/j.jinorgbio.2019.110719.Search in Google Scholar

del Carmen Hernandez-Galindo, M.; Moya-Cabrera, M.; Jancik, V.; Toscano, R. A.; Cea-Olivares, R. Synthesis and structural characterization of organotellurium (IV) complexes bearing ferrocenyldithiophosphonate ligands. The first examples of tellurium dithiophosphonates. J. Organomet.Chem.2014, 772, 280–286. https://doi.org/10.1016/j.jorganchem.2014.09.020.Search in Google Scholar

Deng, X.; Cao, H.; Chen, C.; Zhou, H.; Yu, L. Organotellurium catalysis-enabled utilization of molecular oxygen as oxidant for oxidative deoximation reactions under solvent-free conditions. Sci. Bull.2019, 64, 1280–1284. https://doi.org/10.1016/j.scib.2019.07.007.Search in Google Scholar

dos Santos, S. S.; Cabral, B. N.; Abram, U.; Lang, E. S. Bis (4-pyridyl) ditelluride as starting material for the synthesis of zwitterionic compounds and metal complexes. J. Organomet. Chem.2013, 723, 115–121. https://doi.org/10.1016/j.jorganchem.2012.09.007.Search in Google Scholar

Eisler, D. J.; Robertson, S. D.; Chivers, T. Gold complexes of ditelluridoimidodiphosphinate ligands—Reversible oxidation of Au (I) to Au (III) via insertion of gold into a phosphorus–tellurium bond. Can. J. Chem.2009, 87, 39–46. https://doi.org/10.1139/v08-074.Search in Google Scholar

Engman, L.; Al-Maharik, N.; McNaughton, M.; Birmingham, A.; Powis, G. Thioredoxin reductase and cancer cell growth inhibition by organotellurium compounds that could be selectively incorporated into tumor cells. Bioorg. Med. Chem.2003, 11, 5091–5100. https://doi.org/10.1016/j.bmc.2003.08.021.Search in Google Scholar

Fonseca, S. F.; Lima, D. B.; Alves, D.; Jacob, R. G.; Perin, G.; Lenardao, E. J.; Savegnago, L. Synthesis, characterization and antioxidant activity of organoselenium and organotellurium compound derivatives of chrysin. New J. Chem.2015, 39, 3043–3050. https://doi.org/10.1039/c4nj02329c.Search in Google Scholar

Forge, F.; Beck, J. Double Salts and Mixed Crystals of Tellurium Clusters Te42+/Te82+ and TeCl3+ Ions with Anions based on Molybdenum and Zirconium (Oxy) chlorides. Z. Anorg. Allg. Chem.2018, 644, 1525–1531. https://doi.org/10.1002/zaac.201800052.Search in Google Scholar

Gao, F.; Tang, Y.; Li, Z-H; Pan, F.; Yang, J.; Zhang, Y.-M. A novel regioselective reaction of styrene with magnesium organoselenolates to afford unsymmetrical selenides catalyzed by CuI and l-proline. Tetrahedron Lett.2012, 53, 5688–5690. https://doi.org/10.1016/j.tetlet.2012.08.046.Search in Google Scholar

Gross, M.; Stanciu, E.; Kenigsbuch-Sredni, D.; Sredni, B.; Pinhasov, A. The immunomodulatory tellurium compound ammonium trichloro (dioxoethylene-O, O′) tellurate reduces anxiety-like behavior and corticosterone levels of submissive mice. Behav. Pharmacol.2017, 28, 458–465. https://doi.org/10.1097/fbp.0000000000000319.Search in Google Scholar

Gupta, A.; Deka, R.; Raju, S.; Singh, H. B.; Butcher, R. J. Synthesis of intramolecularly coordinated heteroleptic diorganotellurides and diorganotelluroxides: Isolation of monomeric diorganotelluroxide [{2, 6-(Me2NCH2) 2C6H3} 2TeO] and diorganohydroxytelluronium chloride [{2, 6-(Me2NCH2) 2C6H3} 2Te (OH)] Cl. J. Organomet. Chem.2019, 894, 10–17. https://doi.org/10.1016/j.jorganchem.2019.05.003.Search in Google Scholar

Gupta, A. K.; Deka, R.; Sarkar, A.; Singh, H. B.; Butcher, R. Oxidation behavior of intramolecularly coordinated unsymmetrical diorganotellurides: Isolation of novel tetraorganoditelluronic acids,[RR´ Te (μ-O)(OH) 2] 2. Dalton Trans.2019, 48(29), 10979–10985.10.1039/C9DT01926JSearch in Google Scholar

Gupta, A. K.; Deka, R.; Singh, H. B.; Butcher, R. J. Reactivity of bis [{2, 6-(dimethylamino) methyl} phenyl] telluride with Pd (ii) and Hg (ii): isolation of the first Pd (ii) complex of an organotellurenium cation as a ligand. New J. Chem.2019, 43, 13225–13233. https://doi.org/10.1039/c9nj02469g.Search in Google Scholar

Gusarova, N. K.; Chernysheva, N. A.; Klyba, L. V.; Shagun, V. A.; Yas’ko, S. V.; Smirnov, V. I.; Trofimov, B. A. Mass spectrometry and quantum chemical studies of the reaction of divinyl telluride with secondary phosphine sulfides: synthesis of adducts. J. Organomet. Chem.2013, 745, 126–132. https://doi.org/10.1016/j.jorganchem.2013.07.050.Search in Google Scholar

Habib, A.; Iqbal, M. A.; Bhatti, H. N.; Kamal, A.; Kamal, S. Synthesis of alkyl/aryl linked binuclear silver (I)-N-Heterocyclic carbene complexes and evaluation of their antimicrobial, hemolytic and thrombolytic potential. Inorg. Chem. Commun.2020, 111, 107670. https://doi.org/10.1016/j.inoche.2019.107670.Search in Google Scholar

Halpert, G.; Sredni, B. The effect of the novel tellurium compound AS101 on autoimmune diseases. Autoimmun. Rev.2014, 13, 1230–1235. https://doi.org/10.1016/j.autrev.2014.08.003.Search in Google Scholar

Haque, R. A.; Iqbal, M. A.; Mohamad, F.; Razali, M. R. Antibacterial and DNA cleavage activity of carbonyl functionalized N-heterocyclic carbene-silver (I) and selenium compounds. J. Mol. Struct.2018, 1155, 362–370. https://doi.org/10.1016/j.molstruc.2017.10.092.Search in Google Scholar

Harada, T.; Takahashi, Y. Origin of the difference in the distribution behavior of tellurium and selenium in a soil–water system. Geochim. Cosmochim. Acta2008, 72, 1281–1294. https://doi.org/10.1016/j.gca.2007.12.008.Search in Google Scholar

He, G; Torres Delgado, W.; Schatz, D. J.; Merten, C.; Mohammadpour, A.; Mayr, L.; Ferguson, M. J.; McDonald, R.; Brown, A.; Shankar, K. Coaxing solid‐state phosphorescence from tellurophenes. Angew. Chem. Int. Ed.2014, 53, 4587–4591. https://doi.org/10.1002/anie.201307373.Search in Google Scholar

Hejda, M.; Lork, E.; Mebs, S.; Dostál, L.; Beckmann, J. Intramolecularly Coordinated 2‐Iminomethylphenyltellurium Compounds. Eur. J. Inorg. Chem.2017, 2017, 3435–3445. https://doi.org/10.1002/ejic.201700421.Search in Google Scholar

Hitchcock, P. B.; Lappert, M. F.; Li, G. Complexes containing the [TeCl4X]− moiety (X= Cl or an aryl group). Inorganica Chim. Acta2009, 362, 3982–3986. https://doi.org/10.1016/j.ica.2009.05.037.Search in Google Scholar

Ho, P. C.; Rafique, J.; Lee, J.; Lee, L. M.; Jenkins, H. A.; Britten, J. F.; Braga, A. L.; Vargas-Baca, I. Synthesis and structural characterisation of the aggregates of benzo-1, 2-chalcogenazole 2-oxides. Dalton Trans.2017, 46, 6570–6579. https://doi.org/10.1039/c7dt00612h.Search in Google Scholar

Ho, P. C.; Bui, R.; Cevallos, A.; Lee, L. M.; Jenkins, H. A.; Britten, J. F.; Braga, A. L.; Vargas-Baca, I. Macrocyclic complexes of Pt (ii) and Rh (iii) with iso-tellurazole N-oxides. Dalton Trans.2019, 48, 4879–4886. https://doi.org/10.1039/c9dt00500e.Search in Google Scholar

Hoover, G. C.; Seferos, D. S. Photoactivity and optical applications of organic materials containing selenium and tellurium. Chemical Science2019, 10, 9182–9188. https://doi.org/10.1039/c9sc04279b.Search in Google Scholar

Hou, W.; Zhou, Y.; Rui, J.; Bai, R.; Bhasin, A. K.; Ruan, B. H. Design and synthesis of novel tellurodibenzoic acid compounds as kidney-type glutaminase (KGA) inhibitors. Bioorg. Med. Chem. Lett.2019, 29, 1673–1676. https://doi.org/10.1016/j.bmcl.2019.04.032.Search in Google Scholar

Hulkes, A. J.; Hill, A. F.; Nasir, B. A.; White, A. J.; Williams, D. J. Reactions of μ-alkylidyne complexes with tellurium. Telluroacyl versus μ-telluride formation. Organometallics2004, 23, 679–686. https://doi.org/10.1021/om030614n.Search in Google Scholar

Ibrahim, M.; Hassan, W.; Meinerz, D. F.; Dos Santos, M.; Klimaczewski, C. V.; Deobald, A. M.; Costa, M. S.; Nogueira, C. W.; Barbosa, N. B.; Rocha, J. B. Antioxidant properties of diorganoyl diselenides and ditellurides: modulation by organic aryl or naphthyl moiety. Mol. Cel. Biochem.2012, 371, 97–104. https://doi.org/10.1007/s11010-012-1426-4.Search in Google Scholar

Iqbal, M. A.; Haque, R. A.; Ng, W. C.; Hassan, L. E.; Majid, A. M.; Razali, M. R. Green synthesis of mono-and di-selenium-N-heterocyclic carbene adducts: Characterizations, crystal structures and pro-apoptotic activities against human colorectal cancer. J. Organomet. Chem.2016, 801, 130–138. https://doi.org/10.1016/j.jorganchem.2015.10.023.Search in Google Scholar

Jamier, V.; Ba, L. A.; Jacob, C. Selenium‐and tellurium‐containing multifunctional redox agents as biochemical redox modulators with selective cytotoxicity. Chem. Eur.2010, 16, 10920–10928. https://doi.org/10.1002/chem.201000884.Search in Google Scholar

Kadhum, H. J.; Al-Dewan, M. A.; AL-Jadaan, S. A. Synthesis, charecterization and antioxidant activity of bis [4-(4’-Hydroxy-3’-Methoxy Benzylidene Amino Phenyl)] Telluride. Bas. J. Vet. Res.2014, 13, 36–47.10.33762/bvetr.2014.98792Search in Google Scholar

Kamal, I.; Al-Baage, A., New Organometallic Monomers and Polymers Based on Tellurium Synthesis and Characterization.Search in Google Scholar

Kamal, A.; Iqbal, M. A.; Bhatti, H. N. Therapeutic applications of selenium-derived compounds. Rev. Inorg. Chem.2018, 38, 49–76. https://doi.org/10.1515/revic-2018-0008.Search in Google Scholar

Kamal, A.; Nazari, M.; Yaseen, M.; Iqbal, M. A.; Khadeer, M. B. A.; Majid, A. S. A.; Bhatti, H. N. Green synthesis of selenium-n-heterocyclic carbene compounds: evaluation of antimicrobial and anticancer potential. Bioorg. Chem.2019, 103042. https://doi.org/10.1016/j.bioorg.2019.103042.Search in Google Scholar

Kedarnath, G.; Jain, V. K. Pyridyl and pyrimidyl chalcogen (Se and Te) compounds: a family of multi utility molecules. Coord. Chem. Rev.2013, 257, 1409–1435. https://doi.org/10.1016/j.ccr.2013.01.003.Search in Google Scholar

Klapötke, T. M.; Krumm, B.; Polborn, K.; Schwab, I. Organotellurium (VI) azides and halides. J. Am. Chem. Soc.2004, 126, 14166–14175. https://doi.org/10.1021/ja046637q.Search in Google Scholar

Kociscakova, L.; Senipek, M. I.; Zimcik, P.; Novakova, V. Non-peripherally alkylamino-substituted phthalocyanines: Synthesis, spectral, photophysical and acid-base properties. J. Porphyr. Phthalocya.2019, 23, 427–436, 04n05. https://doi.org/10.1142/s108842461950024x.Search in Google Scholar

Kumar, S.; Engman, L.; Valgimigli, L.; Amorati, R.; Fumo, M. G.; Pedulli, G. F. Antioxidant profile of ethoxyquin and some of its S, Se, and Te analogues. J. Org. Chem.2007, 72, 6046–6055. https://doi.org/10.1021/jo0705465.Search in Google Scholar

Laden, B. P.; Porter, T. D. Inhibition of human squalene monooxygenase by tellurium compounds: evidence of interaction with vicinal sulfhydryls. J. Lipid Res.2001, 42, 235–240.10.1016/S0022-2275(20)31684-9Search in Google Scholar

Lenardão, E.; Borges, E.; Stach, G.; Soares, L.; Alves, D.; Schumacher, R.; Bagnoli, L.; Marini, F.; Perin, G. Glycerol as precursor of organoselanyl and organotellanyl alkynes. Molecules2017, 22, 391. https://doi.org/10.3390/molecules22030391.Search in Google Scholar

Liu, S.; Zeng, X.; Hammond, G. B.; Xu, B. Mild Base Promoted Nucleophilic Substitution of Unactivated sp3‐Carbon Electrophiles with Alkenylboronic Acids. Adv. Synth. Catal.2018, 360, 3667–3671. https://doi.org/10.1002/adsc.201800826.Search in Google Scholar

Lv, L.; Wang, X.; Wang, X.; Yang, L.; Dong, T.; Yang, Z.; Huang, H. Tellurophene-based N-type copolymers for photovoltaic applications. ACS Appl. Mater. Inter.2016, 8, 34620–34629. https://doi.org/10.1021/acsami.6b11041.Search in Google Scholar

Maleki, B.; Babaee, S.; Tayebee, R. Zn (L‐proline) 2 as a powerful and reusable organometallic catalyst for the very fast synthesis of 2‐amino‐4H‐benzo [g] chromene derivatives under solvent‐free conditions. Appl. Organomet. Chem.2015, 29, 408–411. https://doi.org/10.1002/aoc.3306.Search in Google Scholar

Malinski, T. J.; Bergbreiter, D. E. Safer solvents for reactive organometallic reagents. Tetrahedron Lett.2018, 59, 3926–3929. https://doi.org/10.1016/j.tetlet.2018.09.041.Search in Google Scholar

Matsumura, S.; Matsui, Y.; Nagatomo, M.; Inoue, M. Stereoselective construction of anti-and syn-1, 2-diol structures via decarbonylative radical coupling of α-alkoxyacyl tellurides. Tetrahedron2016, 72, 4859–4866. https://doi.org/10.1016/j.tet.2016.06.056.Search in Google Scholar

Mayers, B.; Xia, Y. One-dimensional nanostructures of trigonal tellurium with various morphologies can be synthesized using a solution-phase approach. J. Mater. Chem.2002, 12, 1875–1881. https://doi.org/10.1039/b201058e.Search in Google Scholar

Menon, S. C.; Panda, A.; Singh, H. B.; Patel, R. P.; Kulshreshtha, S. K.; Darby, W. L.; Butcher, R. J. Tellurium azamacrocycles: synthesis, characterization and coordination studies. J. organomet. chem.2004, 689, 1452–1463. https://doi.org/10.1016/j.jorganchem.2003.12.042.Search in Google Scholar

Metre, R. K.; Kundu, S.; Sahoo, D.; Chandrasekhar, V. Reactions of RTeCl3 (R= 2-phenylazophenyl) with Diorganophosphinic Acids. Te–C Bond Cleavage and Stabilization of the Te• O Motif in an Umbrella-Shaped Te5O11P2 Multi-metallacyclic Framework. Organometallics2014, 33, 2380–2383. https://doi.org/10.1021/om5000216.Search in Google Scholar

Misra, S.; Chauhan, A. K.; Srivastava, R. C.; Butcher, R. J.; Duthie, A. Electrophilic substitution of acetyltrimethylsilane with tellurium (IV) halides: A synthetic route to 3-methyl-5-(trimethylsilyl)-1, 2-oxatellurol-1-ium halides. J. Organomet. Chem.2015, 791, 119–123. https://doi.org/10.1016/j.jorganchem.2015.05.055.Search in Google Scholar

Misra, S.; Chauhan, A. K.; Srivastava, R. C.; Butcher, R. J.; Duthie, A. Electrophilic addition/substitution of an alkynyl methyl ketone with tellurium tetrahalides: A novel synthetic approach to telluracyclopentenones. J. Organomet. Chem.2017, 832, 36–41. https://doi.org/10.1016/j.jorganchem.2017.01.012.Search in Google Scholar

Miyasato, M.; Sagami, T.; Minoura, M.; Yamamoto, Y.; Akiba, K. Y. Syntheses and Reactions of Hexavalent Organotellurium Compounds Bearing Five or Six Tellurium(t) Carbon Bonds. Chem. Eur.2004, 10, 2590–2600. https://doi.org/10.1002/chem.200305260.Search in Google Scholar

Mohammadpour, A.; Wiltshire, B. D.; Farsinezhad, S.; Zhang, Y.; Askar, A. M.; Kisslinger, R.; Delgado, W. T.; He, G.; Kar, P.; Rivard, E. Charge transport, doping and luminescence in solution-processed, phosphorescent, air-stable tellurophene thin films. Org. Electron.2016, 39, 153–162. https://doi.org/10.1016/j.orgel.2016.10.001.Search in Google Scholar

Morgan, G. T.; Kellett, R. E. CXL.—Interactions of tellurium tetrachloride and aryl alkyl ethers. Part II. J. Chem. Soc. (Resumed)1926, 129, 1080–1088. https://doi.org/10.1039/jr9262901080.Search in Google Scholar

Munchen, T. S.; Sonego, M. S.; de Souza, D.; Dornelles, L.; Seixas, F. K.; Collares, T.; Piccoli, B. C.; da Silva, F. D. A.; da Rocha, J. B. T.; Quoos, N. New 3’‐Triazolyl‐5’‐aryl‐chalcogenothymidine: Synthesis and Anti‐oxidant and Antiproliferative Bladder Carcinoma (5637) Activity. ChemistrySelect2018, 3, 3479–3486. https://doi.org/10.1002/slct.201800156.Search in Google Scholar

Musalova, M.; Musalov, M.; Potapov, V.; Amosova, S. Methoxytelluration of styrene with tellurium tetrabromide. Russ. J. Org. Chem.2017, 53, 299–300. https://doi.org/10.1134/s1070428017020270.Search in Google Scholar

Musalova, M.; Khabibulina, A.; Potapov, V.; Amosova, S. Stereoselective synthesis of (Z, E)-bis (2-chloroethenyl) tellanes. Russ. J. Org. Chem.2017, 53, 1593–1595. https://doi.org/10.1134/s1070428017100177.Search in Google Scholar

Naz, N.; Saqib, S.; Ashraf, R.; Majeed, M. I.; Iqbal, M. A. Synthesis of new organoselenium compounds: characterization and biological studies. Maced. J. Chem. Chem. En.2020, 39. https://doi.org/10.20450/mjcce.2020.1912.Search in Google Scholar

Nobari, N.; Behboudnia, M.; Maleki, R. Palladium-free electroless deposition of pure copper film on glass substrate using hydrazine as reducing agent. Appl. Surf. Sci.2016, 385, 9–17. https://doi.org/10.1016/j.apsusc.2016.05.033.Search in Google Scholar

Nogueira, C. W.; Zeni, G.; Rocha, J. B. Organoselenium and organotellurium compounds: toxicology and pharmacology. Chem. Rev.2004, 104, 6255–6286. https://doi.org/10.1021/cr0406559.Search in Google Scholar

Nordheider, A.; Woollins, J. D.; Chivers, T. Organophosphorus–tellurium chemistry: from fundamentals to applications. Chem. Rev.2015, 115, 10378–10406. https://doi.org/10.1021/acs.chemrev.5b00279.Search in Google Scholar

Oba, M.; Okada, Y.; Nishiyama, K.; Shimada, S.; Ando, W. Synthesis, characterization and oxidizing properties of a diorgano tellurone carrying bulky aromatic substituents. Chem. Commun.2008, 5378–5380. https://doi.org/10.1039/b811112j.Search in Google Scholar

Oba, M.; Nishiyama, K.; Koguchi, S. Synthesis and properties of tellurinic anhydride–tellurone adducts. Organometallics2013, 32, 6620–6623. https://doi.org/10.1021/om400772d.Search in Google Scholar

Ogra, Y.; Kobayashi, R.; Ishiwata, K.; Suzuki, K. T. Identification of urinary tellurium metabolite in rats administered sodium tellurite. J. Anal. At. Spectrom.2007, 22, 153–157. https://doi.org/10.1039/b613835g.Search in Google Scholar

Ogra, Y.; Kobayashi, R.; Ishiwata, K.; Suzuki, K. T. Comparison of distribution and metabolism between tellurium and selenium in rats. J. Inorg. Biochem.2008, 102, 1507–1513. https://doi.org/10.1016/j.jinorgbio.2008.01.012.Search in Google Scholar

Okio, C. K. Y. A.; Levason, W.; Monzittu, F. M.; Reid, G. Complexes of BX3 with EMe2 (X = F, Cl, Br, I; E = Se or Te): Synthesis, multinuclear NMR spectroscopic and structural studies. J. Organomet. Chem.2017, 848, 232–238, 2017/10/15/. https://doi.org/10.1016/j.jorganchem.2017.08.004.Search in Google Scholar

O’Quinn, G. K.; Rudd, M. D.; Kautz, J. A. Synthesis and characterization of complexes of Te (IV) with sulfur and selenium containing ligands: crystal and molecular structure of trichloro (4-methoxyphenyl) tellurium (IV)· N-methylbenzothiazole-2-(3H)-thione. Phosphorus, Sulfur, and Silicon Relat. Elem.2002, 177, 853–862. https://doi.org/10.1080/10426500210667.Search in Google Scholar

Parent, A. R.; Brewster, T. P.; De Wolf, W.; Crabtree, R. H.; Brudvig, G. W. Sodium periodate as a primary oxidant for water-oxidation catalysts. Inorg. chem.2012, 51, 6147–6152. https://doi.org/10.1021/ic300154x.Search in Google Scholar

Paschoalin, T.; Martens, A. A.; Omori, Á. T.; Pereira, F. V.; Juliano, L.; Travassos, L. R.; Machado-Santelli, G. M.; Cunha, R. L. Antitumor effect of chiral organotelluranes elicited in a murine melanoma model. Bioorg. Med. Chem.2019, 27, 2537–2545. https://doi.org/10.1016/j.bmc.2019.03.032.Search in Google Scholar

Pawar, H. R.; Kamble, N. R.; Kamble, V. T. Chemo selective, room temperature and solvent free synthesis of thio-esters using effective synergistic catalytic system. Methods2019, 12, 1997–2004. https://doi.org/10.31788/rjc.2019.1245381.Search in Google Scholar

Pietrasiak, E.; Baxter, A. F.; Jelier, B.; Santschi, N.; Togni, A. Trifluoromethyl derivatives of benzooxatellurole. Helvetica Chim. Acta2019, 102, e1900079. https://doi.org/10.1002/hlca.201900079.Search in Google Scholar

Poon, J-F; Yan, J.; Singh, V. P.; Gates, P. J.; Engman, L. Regenerable radical-trapping tellurobistocopherol antioxidants. J Org Chem.2016, 81, 12540–12544. https://doi.org/10.1021/acs.joc.6b02450.Search in Google Scholar

Poon, J-F, Exploring Catalytic Tellurium-Based Antioxidants: Synthesis and Evaluation; Acta Universitatis Upsaliensis, 2016.Search in Google Scholar

Potapov, V.; Musalova, M.; Musalov, M.; Rusakov, Y. Y.; Khabibulina, A. G.; Rusakov, I. L.; Amosova, S. V. Regioselective reaction of tellurium tetrabromide with 1-hexene and methanol. Russ. J. Org. Chem.2013, 49, 1703–1704. https://doi.org/10.1134/s1070428013110237.Search in Google Scholar

Potapov, V.; Musalova, M.; Musalov, M.; Amosova, S. Regioselective reaction of tellurium tetrabromide with allyl phenyl ether. Russ. J. Gen. Chem.2014, 84, 2462–2463. https://doi.org/10.1134/s1070363214120214.Search in Google Scholar

Potapov, V. A.; Musalov, M. V.; Musalova, M. V.; Amosova, S. V. Recent advances in organochalcogen synthesis based on reactions of chalcogen halides with alkynes and alkene. Curr Org Chem2016, 20, 136–145.10.2174/1385272819666150810222454Search in Google Scholar

Potapov, V. A.; Musalov, M. V.; Musalova, M. V.; Rusakov, Y. Y.; Khabibulina, A. G.; Rusakova, I. L.; Amosova, S. V. Stereoselective synthesis of E-2-halovinyl tellanes, ditellanes and selenides based on tellurium tetrahalides, selenium dihalides and internal alkynes. J. Organomet. Chem.2018, 867, 300–305. https://doi.org/10.1016/j.jorganchem.2018.02.015.Search in Google Scholar

Prange, A.; Birzele, B.; Hormes, J.; Modrow, H. Investigation of different human pathogenic and food contaminating bacteria and moulds grown on selenite/selenate and tellurite/tellurate by X-ray absorption spectroscopy. Food Control2005, 16, 723–728. https://doi.org/10.1016/j.foodcont.2004.06.010.Search in Google Scholar

Princival, C. R.; Archilha, M. V.; Dos Santos, A. A.; Franco, M. P.; Braga, A. A.; Rodrigues-Oliveira, A. F.; Correra, T. C.; Cunha, R. L.; Comasseto, J. O. V. Stability study of hypervalent tellurium compounds in aqueous solutions. ACS Omega2017, 2, 4431–4439. https://doi.org/10.1021/acsomega.7b00628.Search in Google Scholar

Priyadarsini, K. I.; Singh, B. G.; Kunwar, A. Selenium: chemical biology, toxicology and radioprotection. Biomed. Res. J.2016, 3, 52. https://doi.org/10.4103/2349-3666.240605.Search in Google Scholar

Puntel, L.; Avila, S.; Roos, H D.; Pinton, S. Mitochondrial effects of organoselenium and organotellurium compounds. Curr. Org. Chem.2016, 20, 198–210.10.2174/1385272819666150724234948Search in Google Scholar

Raghavendra, K. P.; Siddagangaiah, P. B.; Upreti, S. Synthesis, spectral characterization of four symmetrical and unsymmetrical organotellurium (II) compounds: O− H… N, CH… π, and CH… O secondary interactions in X‐Ray crystal structures of 4‐MeOC6H4TeCH2CH2CH2N=C (CH3) C6H4‐2‐OH (1) and Te [CH2CH2CH2N=C (CH3) C6H4‐2‐OH] 2 (2). Heteroatom Chem.2015, 26, 313–321. https://doi.org/10.1002/hc.21262.Search in Google Scholar

Rameshkumar, A.; Sivasudha, T.; Jeyadevi, R.; Sangeetha, B.; Ananth, D. A.; Aseervatham, G. S. B.; Nagarajan, N.; Renganathan, R.; Kathiravan, A. In vitro antioxidant and antimicrobial activities of Merremia emarginata using thio glycolic acid-capped cadmium telluride quantum dots. Colloid Surface B2013, 101, 74–82. https://doi.org/10.1016/j.colsurfb.2012.05.034.Search in Google Scholar

Rao, G. K.; Kumar, A.; Singh, M. P.; Singh, A. K. Palladium (II) complex of an organotellurium ligand as a catalyst for Suzuki Miyaura coupling: Generation and role of nano-sized Pd3Te2. J. Organomet. Chem.2014, 749, 1–6. https://doi.org/10.1016/j.jorganchem.2013.08.042.Search in Google Scholar

Revanna, R. H.; Panchangam, R. K.; Bhanu, U.; Doddavenkatanna, S. Synthesis, Characterization and in vitro Antioxidant Activity of New Chiral N-boc Organotellurium Compounds, (CH3) 3OC (O) NHCH (R) C (O) NHCH2-CH2Te-C6H4-4-OCH3, Containing Carbamate and Peptide Groups. J. Brazil. Chem. Soc.2016, 27, 1157–1164.10.5935/0103-5053.20160011Search in Google Scholar

Ruck, M.; Locherer, F. Coordination chemistry of homoatomic ligands of bismuth, selenium and tellurium. Coord. Chem. Rev.2015, 285, 1–10. https://doi.org/10.1016/j.ccr.2014.10.010.Search in Google Scholar

Sacramento, M.; Menezes, L.; Goldani, B.; Perin, G.; Silva, M. S.; da Silva, T. B.; Alves, D. Synthesis of alkynyltellurides mediated by K3PO4 and DMSO. New J. Chem.2019.10.1039/C9NJ01995BSearch in Google Scholar

Sadekov, I. D.; Zakharov, A. V.; Maksimenko, A. A. Diorganyl derivatives of tellurium (IV)(σ-telluranes of R2TeX2 Type). Sulfur Rep.2002, 23, 125–198. https://doi.org/10.1080/0196177021000011149.Search in Google Scholar

Sanford, G.; Walker, K. E.; Fronczek, F. R.; Junk, T. Novel organotellurium heterocycles derived from bis (2‐aminophenyl) ditelluride. J. Heterocycl. Chem.2017, 54, 575–579. https://doi.org/10.1002/jhet.2624.Search in Google Scholar

Satheeshkumar, K.; Raju, S.; Singh, H. B.; Butcher, R. J. Reactivity of selenocystine and tellurocystine: structure and antioxidant activity of the derivatives. Chem. Eur.2018, 24, 17513–17522. https://doi.org/10.1002/chem.201803776.Search in Google Scholar

Ścianowski, J.; Pacuła, A. J.; Wojtczak, A. New and efficient methodology for the synthesis of chiral mono-and ditellurides. Tetrahedron: Asymmetry2015, 26, 400–403.10.1016/j.tetasy.2015.03.004Search in Google Scholar

Singh, A. K.; Kumar, J. S.; Butcher, R. N-{2-(4-methoxyphenyltelluro) ethyl} morpholine (L1) and its platinum (II) and ruthenium (II) complexes. Synthesis and crystal structure of L1 and trans-[PtCl2 (L1) 2]. Inorg. Chim. Acta2001, 312, 163–169. https://doi.org/10.1016/s0020-1693(00)00355-8.Search in Google Scholar

Singh, G.; Singh, A. K.; Sharma, P.; Drake, J. E.; Hursthouse, M. B.; Light, M. E. Hybrid (Te, N) and (N, Te, N) ligands having pyrrolidine ring and their palladium (II) and mercury (II) complexes: synthesis and crystal structures. J.Organomet. Chem.2003, 688, 20–26. https://doi.org/10.1016/j.jorganchem.2003.08.024.Search in Google Scholar

Singh, P.; Chauhan, A. K.; Butcher, R. J.; Duthie, A. Synthesis and structural aspects of 1-naphthyltellurium (IV) trichloride (1), bis (mesityl) tellurium (IV) dichloride (2) and bis (chlorobis (2-thiophenyl) tellurium) oxide (3). Polyhedron2013, 62, 227–233. https://doi.org/10.1016/j.poly.2013.06.044.Search in Google Scholar

Singh, P.; Chauhan, A. K.; Butcher, R. J.; Duthie, A. Electrophilic substitution reactions of 2-acetylpyridine, 2-acetylpyrrole & cyclohexanone: Isolation and molecular structures of novel organotellurium (IV) chlorides. J. Organomet. Chem.2013, 731, 49–54. https://doi.org/10.1016/j.jorganchem.2013.01.029.Search in Google Scholar

Singh, P.; Gupta, A. K.; Sharma, S.; Singh, H. B.; Butcher, R. J. Synthesis and characterization of N, N′, C-bound organotellurium (IV) and organomercury (II) derivatives. Inorg. Chim. Acta2018, 483, 218–228. https://doi.org/10.1016/j.ica.2018.08.016.Search in Google Scholar

Singh, P.; Singh, H. B.; Butcher, R. J. Synthesis and characterization of selenium (I/II) and tellurium (IV) derivatives of amino acids. J. Organomet. Chem.2018, 876, 1–9. https://doi.org/10.1016/j.jorganchem.2018.08.028.Search in Google Scholar

Smith, W. E.; Franklin, D. V.; Goutierrez, K. L.; Fronczek, F. R.; Mautner, F. A.; Junk, T. Organotellurium chemistry: synthesis and properties of 2-acylamino-and 2-arylamino-1, 3-benzotellurazoles. Am. J. Heterocycl. Chem.2019, 5, 49.10.11648/j.ajhc.20190503.11Search in Google Scholar

Soares-Paulino, A. A.; Giroldo, L.; Celante, G.; Oliveira, E.; Santos, S. M.; Mendes, R. F.; Paz, F. A. A.; Fioroto, A. M.; Oliveira, P. V.; Serrano, S. H. Oxidation of tellurium dyes induced by mercury: More insights on the naked-eye and fluorescent Hg2+ detection. Dyes and Pigments2019, 160, 208–216. https://doi.org/10.1016/j.dyepig.2018.07.055.Search in Google Scholar

Sohail, M.; Ashraf, M. Z.; Nadeem, R.; Bibi, S.; Rehman, R.; Iqbal, M. A. Techniques in the synthesis of organometallic compounds of tungsten. Rev. Inorg. Chem.2020, 40, 1–45. https://doi.org/10.1515/revic-2019-0013.Search in Google Scholar

Srivastava, P. C.; Bajpai, S.; Lath, R.; Ram, C.; Srivastava, M.; Butcher, R. J.; Zimmer, M.; Veith, M. Synthesis, spectroscopic characterisation of 1, 1, 2, 3, 4, 5, 6-heptahydro-1, 1-di (carboxylato) telluranes and 1, 3-dihydro-2λ4-benzotellurole-2, 2-diyl dicarboxylates: Crystal structures of 1, 1, 2, 3, 4, 5, 6-heptahydro-1, 1-di (benzoato) tellurane and 1, 3-dihydro-2λ4-benzotellurole-2, 2-diyl dibenzoate. J. Organomet. Chem.2002, 658, 34–42. https://doi.org/10.1016/s0022-328x(02)01594-2.Search in Google Scholar

Srivastava, K.; Panda, A.; Sharma, S.; Singh, B. Telluroxanes: synthesis, structure and applications. J. Organomet. Chem.2018, 861, 174–206, 2018/04/15/. https://doi.org/10.1016/j.jorganchem.2018.02.036.Search in Google Scholar

Sweat, D. P.; Stephens, C. E. A modified synthesis of tellurophene using NaBH4 to generate sodium telluride. J. Organomet. Chem.2008, 693, 2463–2464. https://doi.org/10.1016/j.jorganchem.2008.04.022.Search in Google Scholar

Tanini, D.; Grechi, A.; Dei, S.; Teodori, E.; Capperucci, A. An easy one-step procedure for the synthesis of novel β-functionalised tellurides. Tetrahedron2017, 73, 5646–5653. https://doi.org/10.1016/j.tet.2017.07.061.Search in Google Scholar

Teixeira, M.L.; Menezes, L. R.; Barison, A.; de Oliveira, A. R.; Piovan, L. Investigation of chemical stability of dihalogenated organotelluranes in organic–aqueous media: the protagonism of water. J. Org. Chem.2018, 83, 7341–7346. https://doi.org/10.1021/acs.joc.7b02971.Search in Google Scholar

Topal, G.; Temel, H.; Yavuz, Ö.; Coşkun, M.; Şekerci, M. Preparation of new o-carboxyanilinotellurium (IV) bromides and their dyeing properties. Synth. React. Inorg. Met. Org. Chem.2001, 31, 1097–1107. https://doi.org/10.1081/sim-100105264.Search in Google Scholar

Torres Delgado, W.; Shahin, F.; Ferguson, M. J.; McDonald, R.; He, G.; Rivard, E. Selective placement of bromide and pinacolboronate groups about a tellurophene: new building blocks for optoelectronic applications. Organometallics2016, 35, 2140–2148. https://doi.org/10.1021/acs.organomet.6b00362.Search in Google Scholar

Torubaev, Y.; Pasynskii, A.; Mathur, P. Synthesis and X-ray investigation of novel Fe and Mn phenyltellurenyl-halide complexes:(CO) 3FeBr2 (PhTeBr),(η5-C5H5) Fe (CO) 2 (PhTeI2) and CpMn (CO) 2 (PhTeI). J. Organomet. Chem.2009, 694, 1781–1785. https://doi.org/10.1016/j.jorganchem.2009.01.052.Search in Google Scholar

Torubaev, Y.; Mathur, P.; Pasynskii, A. A. Regio-and stereo-specific addition of organotellurium trihalides to ferrocenylacetylene: Molecular and crystal structure of (Z)-halovinyl organotellurium dihalides. J. Organomet. Chem.2010, 695, 1300–1306. https://doi.org/10.1016/j.jorganchem.2010.02.017.Search in Google Scholar

Torubaev, Y.; Pasynskii, A.; Mathur, P. Organotellurium halides: new ligands for transition metal complexes. Coord. Chem. Rev.2012, 256, 709–721. https://doi.org/10.1016/j.ccr.2011.11.011.Search in Google Scholar

Vargas, F.; Comasseto, J. V. Practical synthesis of chiral β-telluro amines by ring-opening reaction of aziridines. J. Organomet. Chem.2009, 694, 122–126. https://doi.org/10.1016/j.jorganchem.2008.09.025.Search in Google Scholar

Vázquez-Tato, M.; Mena-Menéndez, A.; Feás, X.; Seijas, J. Novel microwave-assisted synthesis of the immunomodulator organotellurium compound ammonium trichloro (dioxoethylene-o, o’) tellurate (AS101). Int. J. Mol. Sci.2014, 15, 3287–3298. https://doi.org/10.3390/ijms15023287.Search in Google Scholar

Vij, P.; Hardej, D. Evaluation of tellurium toxicity in transformed and non-transformed human colon cells. Environ. Toxicol. Pharmacol.2012, 34, 768–782. https://doi.org/10.1016/j.etap.2012.09.009.Search in Google Scholar

Wallschläger, D.; Feldmann, J. 10: Formation, occurrence, significance, and analysis of organoselenium and organotellurium compounds in the environment. Organometallics in environment and toxicology2010, 319–364.10.1039/9781849730822-00319Search in Google Scholar

Wang, L.; Cao, W.; Xu, H. Tellurium‐containing polymers: towards biomaterials and optoelectronic materials. Chem. Nano. Mat2016, 2, 479–488. https://doi.org/10.1002/cnma.201600076.Search in Google Scholar

Wen, K.; Xu, X.; Chen, J.; Lv, L.; Wu, L.; Hu, Y.; Wu, X.; Liu, G.; Peng, A.; Huang, H. Triplet tellurophene-based semiconducting polymer nanoparticles for near-infrared-mediated cancer theranostics. ACS Appl. Mater. Inter.2019, 11, 17884–17893. https://doi.org/10.1021/acsami.9b05196.Search in Google Scholar

Wendler, E. P.; Dos Santos, A. A. The use of butyl organotellurides in the synthesis of natural bioactive compounds. Synlett2009, 2009, 1034–1040.10.1055/s-0028-1088219Search in Google Scholar

Wu, Y.; Yang, L.; Cui, X.; Du, C.; Zhu, Y. Synthesis of novel chiral tellurium complexes by redox reaction of planar chiral cyclomercurated ferrocenylimines with tellurium powder and X-ray crystal structure of [TeCl {C5H5FeC5H3C (CH3)• N-C6H4-4-CH3}]. Tetrahedron: Asymmetry2003, 14, 1073–1077. https://doi.org/10.1016/s0957-4166(03)00163-0.Search in Google Scholar

Wu, Z. G.; Munoz, M.; Montero, O. The synthesis of nickel nanoparticles by hydrazine reduction. Adv. Powder Technol.2010, 21, 165–168. https://doi.org/10.1016/j.apt.2009.10.012.Search in Google Scholar

Wu, Y.; Guo, T.; Qiu, Y. Y.; Lin, Y.; Yao, Y.; Lian, W.; Lin, L.; Song, J.; Yang, H. Inorganic prodrug tellurium nanowire with enhanced ros generation and gsh depletion for selective cancer therapy. Chem. Sci.2019.10.1039/C9SC01070JSearch in Google Scholar PubMed PubMed Central

Yang, H.; Lin, T-P; FoP, G. Telluroether to telluroxide conversion in the coordination sphere of a metal: oxidation-induced umpolung of a Te–Au bond. Organometallics2014, 33, 4368–4373. https://doi.org/10.1021/om5003073.Search in Google Scholar

Yang, L.; Gu, W.; Lv, L.; Chen, Y.; Yang, Y.; Ye, P.; Wu, J.; Hong, L.; Peng, A.; Huang, H. Triplet tellurophene‐based acceptors for organic solar cells. Angew. Chem. Int. Ed.2018, 57, 1096–1102. https://doi.org/10.1002/anie.201712011.Search in Google Scholar

Yaqoob, M.; Gul, S.; Zubair, N. F.; Iqbal, J.; Iqbal, M. A. Theoretical calculation of selenium N-heterocyclic carbene compounds through DFT studies: Synthesis, characterization and biological potential. J. Mol. Struct.2020, 1204, 127462. https://doi.org/10.1016/j.molstruc.2019.127462.Search in Google Scholar

Yarema, M. C.; Curry, S. C. Acute tellurium toxicity from ingestion of metal-oxidizing solutions. Pediatrics2005, 116, e319–e321. https://doi.org/10.1542/peds.2005-0172.Search in Google Scholar

Yoffe, A. Thermal decomposition and explosion of azides. Proc. Roy. Soc. Lond. Math. Phys. Sci.1951, 208, 188–199.10.1098/rspa.1951.0153Search in Google Scholar

Zhang, N.; Fu, N.; Fang, Z.; Feng, Y.; Ke, L. Simultaneous multi-channel hydride generation atomic fluorescence spectrometry determination of arsenic, bismuth, tellurium and selenium in tea leaves. Food Chem.2011, 124, 1185–1188. https://doi.org/10.1016/j.foodchem.2010.07.033.Search in Google Scholar

Zhang, R-F; Nie, J-J; Yan, P-Z; Li, Q.-L.; Zhang, S.-L.; Ma, C.-L. Di-and tri-organotin (IV) complexes derived from aryltelluronic acids: Synthesis, structural characterization and in vitro cytotoxicities. J. Organomet. Chem.2016, 819, 11–19. https://doi.org/10.1016/j.jorganchem.2016.06.009.Search in Google Scholar

Zhang, S.; Zhang, J.; Shi, H.; Gao, Z.; Kou, K. Investigation on the kinetics and thermodynamics of polyacrylonitrile-b-poly (hydroxyethyl acrylate) via organotellurium-mediated living radical polymerization by micro-calorimeter. Thermochim. Acta2019, 682, 178419. https://doi.org/10.1016/j.tca.2019.178419.Search in Google Scholar